Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.
Co-evolution of transcriptional regulatory proteins and their sites of action has been often hypothesized but rarely demonstrated. Here we provide experimental evidence of such co-evolution in yeast silent chromatin, a finding that emerged from studies of hybrids formed between two closely related S...
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doaj-773c08bfcc094af38bae9e895e9e628f2021-07-02T13:42:33ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852010-11-01811e100055010.1371/journal.pbio.1000550Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly.Oliver A ZillDevin ScannellLeonid TeytelmanJasper RineCo-evolution of transcriptional regulatory proteins and their sites of action has been often hypothesized but rarely demonstrated. Here we provide experimental evidence of such co-evolution in yeast silent chromatin, a finding that emerged from studies of hybrids formed between two closely related Saccharomyces species. A unidirectional silencing incompatibility between S. cerevisiae and S. bayanus led to a key discovery: asymmetrical complementation of divergent orthologs of the silent chromatin component Sir4. In S. cerevisiae/S. bayanus interspecies hybrids, ChIP-Seq analysis revealed a restriction against S. cerevisiae Sir4 associating with most S. bayanus silenced regions; in contrast, S. bayanus Sir4 associated with S. cerevisiae silenced loci to an even greater degree than did S. cerevisiae's own Sir4. Functional changes in silencer sequences paralleled changes in Sir4 sequence and a reduction in Sir1 family members in S. cerevisiae. Critically, species-specific silencing of the S. bayanus HMR locus could be reconstituted in S. cerevisiae by co-transfer of the S. bayanus Sir4 and Kos3 (the ancestral relative of Sir1) proteins. As Sir1/Kos3 and Sir4 bind conserved silencer-binding proteins, but not specific DNA sequences, these rapidly evolving proteins served to interpret differences in the two species' silencers presumably involving emergent features created by the regulatory proteins that bind sequences within silencers. The results presented here, and in particular the high resolution ChIP-Seq localization of the Sir4 protein, provided unanticipated insights into the mechanism of silent chromatin assembly in yeast.http://europepmc.org/articles/PMC2994660?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Oliver A Zill Devin Scannell Leonid Teytelman Jasper Rine |
spellingShingle |
Oliver A Zill Devin Scannell Leonid Teytelman Jasper Rine Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly. PLoS Biology |
author_facet |
Oliver A Zill Devin Scannell Leonid Teytelman Jasper Rine |
author_sort |
Oliver A Zill |
title |
Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly. |
title_short |
Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly. |
title_full |
Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly. |
title_fullStr |
Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly. |
title_full_unstemmed |
Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly. |
title_sort |
co-evolution of transcriptional silencing proteins and the dna elements specifying their assembly. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Biology |
issn |
1544-9173 1545-7885 |
publishDate |
2010-11-01 |
description |
Co-evolution of transcriptional regulatory proteins and their sites of action has been often hypothesized but rarely demonstrated. Here we provide experimental evidence of such co-evolution in yeast silent chromatin, a finding that emerged from studies of hybrids formed between two closely related Saccharomyces species. A unidirectional silencing incompatibility between S. cerevisiae and S. bayanus led to a key discovery: asymmetrical complementation of divergent orthologs of the silent chromatin component Sir4. In S. cerevisiae/S. bayanus interspecies hybrids, ChIP-Seq analysis revealed a restriction against S. cerevisiae Sir4 associating with most S. bayanus silenced regions; in contrast, S. bayanus Sir4 associated with S. cerevisiae silenced loci to an even greater degree than did S. cerevisiae's own Sir4. Functional changes in silencer sequences paralleled changes in Sir4 sequence and a reduction in Sir1 family members in S. cerevisiae. Critically, species-specific silencing of the S. bayanus HMR locus could be reconstituted in S. cerevisiae by co-transfer of the S. bayanus Sir4 and Kos3 (the ancestral relative of Sir1) proteins. As Sir1/Kos3 and Sir4 bind conserved silencer-binding proteins, but not specific DNA sequences, these rapidly evolving proteins served to interpret differences in the two species' silencers presumably involving emergent features created by the regulatory proteins that bind sequences within silencers. The results presented here, and in particular the high resolution ChIP-Seq localization of the Sir4 protein, provided unanticipated insights into the mechanism of silent chromatin assembly in yeast. |
url |
http://europepmc.org/articles/PMC2994660?pdf=render |
work_keys_str_mv |
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